FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in quality control and compliance for raw materials and finished products, with a strong focus on FDA regulations and ISO standards. Proven ability to lead quality initiatives, manage non-conformances, and facilitate cross-functional collaboration.
Highest-signal resume keywords
FDA 21 CFR Part 111/117 KnowledgeISO/IEC 17025 Standards KnowledgeQuality Control ManagementCAPA ManagementMicrobiological Testing Coordination
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Quality Compliance ManagementNon-Conformance ReviewTesting Protocols ManagementContinuous Improvement InitiativesLaboratory Testing CoordinationMaterial Review ProcessesComplaint InvestigationQC Record MaintenanceSpecification ApprovalLean Initiatives Implementation
Soft Skills
LeadershipTrainingCollaborationCommunicationProblem-Solving
Industry Keywords
Quality ControlRegulatory InspectionsContract Manufacturer OversightProduct Launch SupportQC Training
About the role
Key responsibilities & impact- Ensure quality and compliance of raw materials and finished products manufactured by external partners
- Oversee quality control activities at contract manufacturers
- Implement quality programs and drive continuous improvement initiatives
- Manage daily quality compliance and ensure timely product release
- Review non-conforming materials and assist with complaint investigations
- Review supplier and laboratory Certificates of Analysis for accuracy and specification compliance
- Facilitate testing and release or rejection of raw material and finished product samples
- Provide onsite quality support during new product launches
- Lead the material review board and manage disposal of non-conforming, expiring, damaged, and returned products
- Maintain QC records for audits and regulatory inspections
- Manage and approve finished product specifications and testing protocols
- Coordinate third-party laboratory testing and evaluate external laboratories
- Validate new testing methods or procedures when required
- Collaborate with Operations, QA, Regulatory, R&D, logistics, and Quality teams
- Implement lean or efficiency-focused initiatives to optimize QC operations
- Support cross-functional QC training and monitor industry and regulatory changes
Requirements
What you’ll need- Experience requirements are not specified in the posting
- Knowledge of FDA 21 CFR Part 111/117 requirements for foods and dietary supplements
- Knowledge of ISO/IEC 17025 standards or equivalent
- Ability to coordinate microbiological, chemical, analytical, and stability testing
- Ability to manage contract manufacturer quality control activities
- Ability to lead and train virtual QC team members
- Ability to manage CAPAs, non-conformances, deviations, complaints, and material review processes
